HIV-HCV Co-infection Slide Kit

HIV-Hepatitis CVirus Co-infection:
An Evolving Epidemic
Marina B. Klein, MD, MSc, FRCP(C)
Division of Infectious Diseases and ChronicViral Illness Service
McGill University Health Centre

HCV Genotype
 Genotypes 1-6
 62% genotype 1 in Canada
 1, 3 more in IDUs
 Genotypes 2a and 5 are more frequent
in patients previously exposed to
multiple injections, surgery, or
transfusions
 Type 4 more in African immigrants
 Existence of several genotypes in
Canada despite low prevalence of HCV
reflects the diversity of the population
and active immigration
 Most important predictor of IFN
treatment response
 Does not predict amount of liver
damage
1
62%
2
14%
3
14%
4
4%
5
4%
6
2%
AndonovA, Chaudhary RK. J Clin Microbiol ,1994.

Hepatitis C: A Worldwide Epidemic
Estimated ~ 170 million (3.1%) globally (2003)
1, 2, 3 1
1, 3
1,3
1
Worldwide: 6
3
4
4
4
4,5
Asia: 63
Europe
8.9 million
(1.03%)
The Americas
13.1 million
(1.7%)
Africa
31.9 million
(5.3%)
SoutheastAsia
32.3 million
(2.15%)
Western Pacific
62.2 million
(3.9%)
Eastern
Mediterranean
21.3 million
(4.6%)
Most CommonGenotype
World HealthOrganization. HepatitisC: global prevalence: update. 2003.
Farci P, et al. Semin Liver Dis. 2000.Wasley A, et al. Semin Liver Dis. 2000.
Remis, for the Public HealthAgency of Canada. Modeling the Incidence and Prevalence of HepatitisC
Infection and its Sequelae in Canada, 2007. Unpublished data, 2009.
Canada
242,000
(0.7%)

HCV: A Global Public Health Concern
HIV
HBV + HCV
Measles
RSV, Rota
Flu
Dengue
HPV
West Nile
SARS
Ebola
Polio
Hanta
7
6
5
4
3
2
1
Log10GlobalDeathRate
Tobacco
Malaria
Road accidents
Non-HIVTB
Hospital infection
Suicide
vCJD
Global Death Rate
Caused byViruses Other Causes
Adapted by permission from Macmillan Publishers Ltd: Nature Medicine.
Weiss RA, et al; copyright 2004.

Morbidity and Mortality for the top 20
pathogens in ON, ranked by disease burden
OnBOIDS, Dec 2010
HepatitisC virus
Streptococcus pneumoriae
Human papillomavirus
Hepatitis B virus
Escherichia coli
HIV/AIDS
Staphylococcus aureus
Influenza
Clostridium difficile
Rhinovirus
Respiratory syncytial virus
Parainfluenza virus
Group B steptococcus
GroupA steptococcus
Haemophilus influenza
Tuberculosis
Legionella
Chlamydia
Adenovirus
Gonorrhea
Years of Life Lost (YLL)
Year-Equivalents of Reduced Functioning
(YERF)
0 2,000 4,000 6,000 8,000 10,000
Health Adjusted LifeYears

Estimated numbers of Co-infected
persons (worldwide)
Canada: 30% HIV+
(est. 12-15,000) co-
infected

Prevalence of HCV among
HIV seropositives
8
41
56 60
80
0
10
20
30
40
50
60
70
80
90
Urban
Clinic
Hemophiliacs*MSM Prisons IDU
Remis R. HealthCanada Report, 2001.

IDU and HIV
Public Health Agency of Canada, 2010

HIV Infection: RecentTrends
Diagnosis of HIV Infection in Canada, 1998 and 2008
Source: ©Statistics Canada & PHAC/Office of Public Health Practice, July 2010
Rate (per 100,00 population) of Diagnoses of HIV Infection in
Canada, 1998 and 2008 (both sexes, ages >= 15)

Saskatchewan:
An Emerging Epidemic
HIV Cases by Selected Self-reported Ethnicity in Saskatchewan, 2000 to 2009
Ministry on Health-PHB, 2010

Reported cases of acute HCV infections among HIV-
positive men who have sex with men and prevalence
of chronic HCV/HIV infection.
Vogel, Rockstroh. J Antimicrob Chemother, 2010

 IDU in 73%
 Sexual transmission in 18%
of whom 92% were HIV+.
Acute HCV:
Importance ofTransmission networks
Matthews. Clin Inf Dis, 2011

Increased Risk of Cirrhosis and ESLD in
HIV/HCV-Coinfected Patients
RR of for end-stage liver disease: 2.92 (95% CI, 1.70-5.01).
Graham et al. Clin Infect Dis, 2001
Relative Risk (95% Cl)
0.76 1.0 2.07 10.83 0.61 1.0 6.14 10 175.32
Makis
Soto
Combined
Benhamou
Pol
Eyster
Telfer
Makris
A
Lesens
Combined
B

Predicted Future Prevalence of HCV in
the United States
Armstrong et al. Hepatology, 2000
PrevalenceofHCVInfection
4.0%
2.0%
3.0%
1.0%
0.0%
Year
1960 1970* 1980 1990 2000 2010 2020 2030
Total Infected HCC
Cirrhosis

Projected liver-related outcomes:
Population 242,521
0
100
200
300
400
500
600
700
800
900
1967 1972 1977 1982 1987 1992 1997 2002 2007 2012 2017 2022 2027
Cirrhosis
Death
HCC
Decompensation
Cases
Remis R. Public Health Agency of Canada, 2007

Study Setting:
The Canadian Co-infection Cohort
 Multi-site prospective
cohort of HIV-infected
persons with chronic HCV
infection or evidence of
HCV exposure
 Between 2003 and the
end of 2012, 1020 persons
were enrolled from 16 sites
 Follow-up visits take
place every 6 months
 Participants fill out a
questionnaire and provide
blood for laboratory
analysis

Mortality in the Canadian Co-infection
Cohort Study
SMR: 17.08 (95% CI; 12.83, 21.34)
Cause of death N %
ESLD 18 29
OVERDOSE 15 24
CANCER 6 10
AIDS 3 5
OTHERS
(infections/trauma)
9 15
UNKNOWN 11 18
Total 62 100
0
2
4
6
8
10
12
14
Deaths/100Person-Years
Age Categories
Death RateTotal
Total Population
Total CCC
Klein. HIV Medicine, 2012

How to reduce burden of HCV in HIV
infected persons?
 Testing
 Estimates that in US only 30% of chronic HCV are aware of their infection;
 Among HIV infected persons this is probably much lower as routine
screening for HCV is recommended
 Harm reduction, counselling and services
 Safe injection and infection control practices
 Need to increase general knowledge among patients and
physicians and referral to HCV care and services as HCV is
often not prioritized
 Treatment
 Clear evidence that successful HCV treatment leads to reduced disease
burden (e.g. Reduces rates of cirrhosis, ESLD and HCC)
 ?Treatment as prevention

High Rates among incarcerated
Populations
 Among those ever tested for
HCV, 31% reported being
positive
 This self-reported rate of HCV
infection is approximately 39
times greater than the rate of
0.7% in the Canadian
population
 Aboriginal women reported
the highest rate: 49%, more
than 50% greater than the
rates among non-Aboriginal
women (30%) and all men
(30.8%)
CorrectionalServices 2010 No R-211
0
10
20
30
40
50
60
Overall
Non-Aboriginal
Aboriginal
HIV HCV
% EverTold they had HIV or HCV

A minority of co-infected patients
initiate treatment
US:
Overall only 20%
initiate treatment in
the HOPS cohort
Canada:
 1.1% (15 of 1360) initiated treatment for HCV from January
2000 to December 2004 in a BC inner city cohort (Grebely, J
Viral Hepatitis, 2009)
 Canadian Co-infection Cohort: 16% already treated at baseline
and 13% initiate follow-up (total: 29% in 2010)

HIV-HCV Epidemiology: Summary
 Co-infection infection occurs worldwide
 In Canada, HCV is strongly associated with IDU and the
correctional system especially in aboriginals
 Newly identified risk among high risk MSM especially HIV+
 Looming epidemic of ESLD and liver related death
 Reducing the burden of HCV related morbidity and
mortality will require enhanced testing, referral for
evaluation and HCV treatment initiation

Management of HIV infection
in HIV/HCV co-infected patients
Mark Hull, MD, MHSc, FRCPC
Division of AIDS
University of British Columbia

Objectives
 Review the effects of antiretroviral therapy (cART) on HCV
natural history
 ART regimen choice in co-infected patients:
 Risk of hepatotoxicity
 Amelioration of hepatic fibrosis
 Drug-drug interactions with HCV therapy

Introduction
 HIV co-infection negatively affects HCV disease
progression:
 Decreased rates of spontaneous clearance in those with pre-
existing HIV
 ~10% will clear acute infection
 Higher HCV viral loads, regardless of genotype
 Impacts treatment response to pegylated interferon and
ribavirin dual combination regimens
Thomas et al. JAMA 2000.
Sherman et al. J Clin Microbiol,1993.

Introduction
 HIV co-infection negatively affects HCV disease
progression:
 Faster progression to cirrhosis in individuals with
untreated HIV infection
 Mean estimated interval to cirrhosis as short as 6.9 yrs vs.
23.2 yrs
 This translates into higher risk of complications
 Meta-analysis of 8 studies found co-infection had increased
risk of 6.14 for decompensated liver disease
Soto et al. J Hepatol, 1997.
Graham et al. CID, 2001.

Introduction
 Management of HIV infection requires consideration of :
 1. Effects of antiretroviral therapy (ART) on HCV disease
progression
 Early initiation of ART may be necessary
 2. Optimizing ART regimen selection
 Risk of hepatotoxicity
 Potential effects on fibrosis progression
 Drug-drug interactions with HCV therapeutic agents

Effects of cART on HCV disease
progression
 Control of HIV viremia may lead to slower rates of fibrosis
progression
 Co-infected individuals undergoing liver biopsy with HIV viral
load (pVL) >400 copies/mL had faster fibrosis progression
rates than those with pVL <400 copies/mL
 Duration of cART-related pVL suppression associated with
decreased hepatic fibrosis
Brau et al. J Hepatol, 2006.
Tural et al. JViral Hepatitis, 2003.

cART decreases HCV liver-related
mortality
 Bonn cohort (1990-2002)
 285 HIV-HCV co-infected
patients
 93 received cART
(HAART), 55 dual
nucleosides (ART) and 137
received no ARVs
 Liver-related mortality rates
per 100 person-years
 cART: 0.45
 Dual therapy: 0.69
 No therapy: 1.70
Qurishi et al. Lancet 2003.

cART decreases liver-related mortality
 Prospective cohort of 472
HIV-infected patients
 72 HBV+, 256 HCV+
 8343 patient-months of
followup
 41% of overall mortality due
to liver-related deaths
 Use of 0-2 ART agents vs.
cART associated with
liver-related mortality
(Relative Risk 2.9, 95% CI
1.3 – 6.7)
Multivariate analysis of factors associated
with liver mortality: protective effect of cART
Bonacini et al. AIDS, 2004.

IAS-USA
Guidelines
2012
US DHHS
Guidelines
2012
British HIV
Association
Guidelines
2012
European
AIDSClinical
Society
Guidelines
2012
HCV co-
infection
ART
regardless of
CD4 cell
count
ART
regardless of
CD4 cell
count
ART if CD4 <
500 cells/mL
ART if CD4 <
500 cells/mL
>500 –
consider if
HCV therapy
not feasible
Grade of
evidence
BIIa BII IC

Incidence of Hepatic Decompensation
despite cART
ART-Treated
HIV/HCV-Coinfected
HCV-Monoinfected
Log-rank
p<0.001
* Based on competing risk regression analysis. Lo Re. IAS 2012.AbstractWEAB0102

Antiretroviral therapy-related
hepatotoxicity
 Initiation of cART is associated with increased risk of
hepatotoxicity in co-infected individuals.
 The incidence of Grade 3 or 4 hepatotoxicity has been
estimated to be between 2-18% in observational studies
 Additional risk factors include alcohol or substance use, older
age and in some studies genotype 3 HCV
Nunez. Hepatology, 2010.
Nunez et al. JAIDS, 2002.

Mechanisms of liver toxicity
Figure from Nunez. J Hepatology, 2006.

hepatotoxicity
 Most reports of hepatotoxicity originate in the early cART
era (1996-2002)
 Early protease inhibitors associated with risk of
hepatotoxicity
 In particular high-dose ritonavir
 Nevirapine > efavirenz
Sulkowski et al. JAMA, 2000.
Aceti et al. JAIDS, 2002.
Sulkowski et al. Hepatology, 2002.
Martin-Carbonero et al. HIV ClinTrials, 2003.

hepatotoxicity
 Successful HCV therapy
associated with decreased
risk of subsequent ART
hepatotoxicity
 Cohort of 132 co-infected
individuals
 33% achieved SVR
 Lower yearly incidence of
hepatotoxicity in those
with SVR (3.1% vs. 12.9%)
Labarga et al. JID, 2007.

Current antiretroviral regimens in co-
infected patients
 Current first and second line regimens appear well-
tolerated in HCV co-infected patients
 Atazanavir/ritonavir
 Raltegravir
 Rilpivirine
 Etravirine
 Darunavir/ritonavir
Absalon et al. J Int AIDS Soc, 2008.
Rockstroh et al. ICAAC, 2012 Abstract 1297.
Nelson et al. JAC, 2012.
Clotet et al. JAC, 2010.
Rachlis et al. HIV ClinTrials, 2007.

cART and HCV therapy
 DDI:
 increased risk of mitochondrial toxicity
 Increased risk of hepatic decompensation if cirrhotic
 D4T:
 increased risks of mitochondrial toxicity/lactic acidosis while
on ribavirin
 AZT:
 increased risk of anemia
 Concomitant need for ribavirin dose reduction
 Decreased SVR
Alvarez et al. JViral Hepatitis, 2006.
Fleischer et al.Clin Infect Dis, 2004.
Bani-Sadr et al. J Infect Dis, 2008.

cART and HCV therapy
 Abacavir: ? interaction with ribavirin with lower HCV SVR
 Retrospective review of the RIBAVIC trial: OR 4.92 (95% CI
1.50-16.06) for lower EVR
 Not seen in analyses of SVR in a cohort treated with weight-
based dosing
Bani-Sadr et al. JAIDS, 2007.
Laufer et al.AntiviralTherapy, 2008.

cART and HCV PI interactions
ARV Telaprevir Boceprevir
Raltegravir ↔ ↔
Efavirenz ↓Telaprevir AUC
Needs dose of 1125mg
q8hr
↓ 20% BOC AUC/Cmin
Atazanavir/r ↓ 20%TPVAUC
↑17%ATV AUC
↓35%ATV AUC
Lopinavir/r ↓54%TPV AUC ↓45% BOCAUC
↓34% LPVAUC
Darunavir/r ↓ 35%TPV AUC
↓40% DRVAUC
↓32% BOC AUC
↓44% DRVAUC

Novel considerations for cART choice in
co-infection
 Potential decrease in fibrosis progression with switch from
PI to raltegravir
 Ongoing clinical trial
 ClinicalTrials.gov identifier: NCT01231685
 Maraviroc may modulate chemokine pathways associated
with fibrosis
 Preliminary studies underway
Macias et al. Eur J Clin Microbiol Infect Dis, 2012.
Nasta et al. IAS, 2010AbstractWEAB0105

Conclusions
 Untreated HIV infection is associated with rapid
progression of hepatic fibrosis and cirrhosis risk.
 Initiating cART may slow progression of hepatic disease
 But increased risk for hepatic disease remains higher than
mono-infected patients
 Current guidelines support early cART initiation in
HIV/HCV patients
 In those with CD4 count >500 strong consideration should be
given to HCV therapy prior to cART

Conclusions
 cART use may increase risk of hepatoxicity
 Prior successful HCV therapy lowers this risk
 Selection of cART regimen should take into account future
HCV therapy and risk of drug-drug interactions

Management of HCV in
Co-Infected Patients
Marie-LouiseVachon, MD, MSc
Division of Infectious Diseases
Centre Hospitalier Universitaire de Québec

Management of HCV
in Co-Infected Patients
 Prevention and counselling
 Baseline laboratory testing
 All patients should be considered for HCV treatment
 Treatment recommendations for HCV genotype 1
infection
 Monitoring during therapy
 Side effect management
 Resistance issues

Prevention and Counselling: What
patients should be told
 Avoid alcohol
 Maintain healthy diet and weight
 Use precautions to prevent transmission of HCV (and HIV)
to others and reinfection
 Get vaccinated against hepatitis A virus (HAV) and
hepatitis B virus (HBV) if susceptible
 Give a complete list of
medications, vitamins, supplements and herbs you are
currently taking to your doctor

Baseline LaboratoryTesting
 Virological tests to confirm
and type HCV infection
 Anti-HCV
 HCV RNA
 HCV genotype
 Baseline blood tests
 CBC with differential
 CD4/CD8 counts
 Liver enzymes and function
tests (ALT, AST, ALP, GGT,Tot
and direct bili, albumin, INR)
 Glucose and insulin, creatinine
 AFP
 Liver Imaging
 Abdominal ultrasound
 Liver fibrosis assessment
 FibroScan
 Biomarker panel
 Liver biopsy
 Other
 Screen for HBV and HAV
immunity
 Tests to exclude other liver
disease
 Tests to diagnose extrahepatic
manifestations of HCV
 IL28B

FibroScan® and serum biomarkers
for fibrosis assessment
 FibroScan ® (transient
elastography)
 Health Canada-approved
 Non-invasive
 Fast
 Can be done during first
patient’s visit
 High sensitivity to exclude
cirrhosis
 Validated in HIV/HCV co-
infected patients
 Serum biomarkers
 APRI
 FIB-4
 Forns index
 others
Liver biopsy is helpful when there is discordant or indeterminate results with
non-invasive techniques and to diagnose other causes of liver disease.

All patients with HIV/HCV co-infection
should be considered for HCV therapy
 HCV PI in association with pegIFN and RBV has been
approved for treatment of genotype 1 HCV mono-
infection
 Safety and efficacy in HIV-infected patients are largely
unproven and regulatory approval is pending, but
preliminary data are encouraging
 Decisions to use or withhold HCV PIs in HIV/HCV co-infected
persons depend on multiple considerations
 Contraindications to pegIFN and RBV therapy apply with
the use of HCV PI

Considerations prior to decision to
use or withold HCV treatment
 HCV eradication is associated with decreased morbidity and mortality
 Liver fibrosis progresses more rapidly in HIV co-infected patients
 Priority is given to patients with advanced fibrosis and cirrhosis
 Higher success rates are achieved in patients with positive predictors of SVR
 Consider treating patients with IL28B CC genotype, low viral load (<400 000
IU/ml), naïve or prior relapsers, even if no or low fibrosis stage
 Patient’s motivation
 Now may be a good time to treat for some patients (e.g. young woman with mild
fibrosis who wishes to become pregnant in the future)
 Well-controlled HIV is desired before starting HCV treatment
 Patients with well-controlled HIV respond better to HCV treatment and higher CD4
counts facilitate management during HCV treatment. For patients with low CD4 counts
(<200 cells/mm3), if possible, ART should be initiated and HCV treatment delayed until
HIV RNA is undetectable and CD4 counts have increased
 Drug-drug interactions between HCV PIs and ART should be assessed: overall limited data
available
 Liver transplantation is not widely available and not highly successful in HIV co-infected
 Poor side effect profile associated with HCV PIs and new anti-HCV drugs are being
developed

Treatment Options for HCV Genotype 1 Patients
co-infected with HIV: DHHS Guidelines
Recommendations on use of boceprevir or telaprevir in HIV/HCV
genotype 1 co-infected patients
DHHSGuidelines, 2012.
*These recommendations may be modified as new drug interaction and clinical trial information become available.
Patient Group Recommendation*
Patients not onART Use either boceprevir or telaprevir
Patients receiving RAL
+ 2 NRTIs
Use either boceprevir or telaprevir
Patients receiving
ATV/r + 2 NRTIs
Use telaprevir at the standard dose.
Do not use boceprevir.
Patients receiving EFV
+ 2 NRTIs
Use telaprevir at increased dose of 1,125 mg
every 7-9 hours.
Do not use boceprevir.

Proposed treatment algorithm: telaprevir in
patients with HIV/HCV co-infection
Until more data are available, a 48 week treatment duration is recommended
for all HIV infected patients using week 4, 12 and 24 futility rule time
points, without RGT.
Peg-IFN : peginterferon; RBV : ribavirine; RGT: response-guided therapy
* Stop treatment at these timepoints because of futility in patients with HCV RNA > 1000 IU/mL at week 4 or 12
or a detectable HCV RNA at week 24.
End of
treatmen
t
Undetectable
HCV RNA
PEG-IFN/RBV
Week 4* Week 24* Week 4812*
Peg-IFN/RBV
Telaprevir +
Peg-IFN/RBV
8*0

Add boceprevir at
end of week 4
Proposed treatment algorithm: boceprevir in
patients with HIV/HCV co-infection
Until more data are available, a 48 week treatment duration is recommended for all
HIV infected patients using week 12 and 24 futility rule time points, without RGT.
52
Peg-IFN : peginterferon; RBV : ribavirine; RGT: response-guided therapy
* Stop treatment at these time points because of futility in patients with HCV RNA >100 IU/ml at week 12 or a
detectable HCV RNA at week 24.
End of
treatment
HCV RNA
undetectable
PEG-IFN/RBV
Week Week 24* Week 4812*
Boceprevir + Peg-IFN/RBVPeg-IFN
RBV
840

Monitoring during HCV treatment
What to monitor
 HCV RNA, quantitative
 HCV RNA, qualitative
 Other laboratory tests
 CBC with differential, liver
panel, biochemistry,TSH, CD4
cell count, HIV viral load, and
AFP if cirrhotic
When to monitor
Telaprevir: Week 0,4,8, and 12
Boceprevir: Week 0 and 12
Telaprevir: Week 24 and 48
Boceprevir: Week 24 and 48
CBC weekly for the first 4 weeks of PI
use, every other week until week 12 and
every month thereafter. Use clinical
judgement. Liver panel, CD4 count, .
biochemistry andTSH monthly.
HIV load every 4-12 weeks, AFP every 6
months if cirrhotic.

Testing during HCV treatment with
telaprevir of HIV co-infected patients
Week
Test
0 1,2,3 4 6 8 10 12 16 20 24 28-
44
48
HCV
RNA
quant
X X X
HCV
RNA
qual
X X
CBC X X X X X X X X X X X X
CD4+ X X X X X 36 X
HIV
RNA
X X X X 36 X
Liver
+ bio
X X X X X X X X X
TSH X X X X X X X X X
AFP X X X

Testing during HCV treatment with
boceprevir of HIV co-infected patients
Week
Test
0 2 4 5,6,7 8 10 12 16 20 24 28-44 48
HCV
RNA
quant
X X
HCV
RNA
qual
X X
CBC X X X X X X X X X X X X
CD4+ X X X X X 36 X
HIV
RNA
X X X X 36 X
Liver
+ bio
X X X X X X X X X
TSH X X X X X X X X X
AFP X X X

Side effect management
 The most frequent adverse events reported in the clinical
trials are
 Telaprevir: Rash, pruritus, anemia and ano-rectal discomfort
 Boceprevir: Anemia and dysgueusia
 Same side effect management in co-infected as in HCV
mono-infected
 Anemia can be severe and develop rapidly
 Ribavirin dose reduction in HCV mono-infection does not
impact SVR rates

HCV Protease Inhibitors and resistance
Higher HCV viral load in HIV/HCV co-infected patients suggests
higher risk for resistance development
 Patient adherence to q7-9 hours schedule of boceprevir and telaprevir
 Strict adherence to futility rules
 Boceprevir and telaprevir have the same resistance pattern. Patients
who fail HCV PI therapy should not be retreated with the same or the
other protease inhibitor
 Not every patient needs to be treated right away: treatment can be
deferred in those with no or mild fibrosis or unmotivated patients
 Other anti-HCV treatment classes are being evaluated in clinical trials
that will be active against PI failures

Summary: Management of HCV
in co-infected patients
 Baseline blood, imaging and fibrosis assessment is
important to characterize HCV infection and plan HCV
treatment
 PegIFN/RBV combination has low efficacy but SVR
significantly increases outcomes
 Hepatitis C protease inhibitors in combination
with PegIFN/RBV increase SVR
 Phase II and III trials under way
 Significant drug-drug interactions with ART

HCVTherapy:
Direct Acting Antiviral Agents
in Co-Infected Individuals
Curtis Cooper, MD, FRCPC
Faculty of Medicine, Division of Infectious Diseases
University of Ottawa

Key Peg-Interferon and Ribavirin Studies
in HIV-HCV Co-Infection
 APRICOT (Dietrich et al.)
 95 centers, 19 countries (Canada 33 patients)
 Academic based
 RIBAVIC (Perrone et al.)
 ANRS (French National Study Group)
 Community based
 ACTG 5071 (Chung et al.)
 US Cooperative group
 21 US community based sites

APRICOT (Dietrich)
Primary endpoint: loss of serum HCV-RNA 24 weeks post-treatment.
3MIUTIW (48 wks)
IFN alfa-2a + ribavirin 800 mg/daily
N=285
N=286
N=511
24 weeks
48 weeks
PEG IFN alfa-2a + Placebo
PEG IFN alfa-2a + ribavirin 800 mg/daily
180 g QW (48 wks)
Follow-up
Endpoint
N=289
Screening
180 g QW (48 wks)

8%
21%
38%
7%
14%
29%
0%
10%
20%
30%
40%
50%
60%
IFN alfa-2a + RBV PEG-IFN alfa-2a (40
kDa) + Placebo
PEG-IFN alfa-2a (40
kDa) + RBV
Virologic Response* – End ofTreatment
vs End of Follow-up (Genotype 1)
%Response
* Defined as <50 IU/mL HCV RNA
End of treatment SVR

27%
57%
64%
20%
36%
62%
0%
10%
20%
30%
40%
50%
60%
70%
IFN alfa-2a + RBV PEG-IFN alfa-2a (40 kDa)
+ Placebo
PEG-IFN alfa-2a (40 kDa)
+ RBV
Virologic Response* – End ofTreatment
vs End of Follow-up (Genotype 2 and 3)
%Response
* Defined as <50 IU/mL HCV RNA
End of treatment SVR

Withdrawal fromTreatment
0%
5%
3%
14%
12% 12%
24%
15%
10%
0%
5%
10%
15%
20%
25%
30%
IFN alfa-2a + RBV PEG-IFN alfa-2a (40 kDa)
+ Placebo
PEG-IFN alfa-2a (40 kDa)
+ RBV
Laboratory abnormality Adverse event Non-safety
%ofPatients

5%
15%
0%
20%
40%
IFN 3 MIUTIW + RBV
800
PEG 1.5 + RBV 800
%SVR
RIBAVIC:
ITT SVR Genotype 1

RIBAVIC: Safety
Treatment Discontinuation:
IFN + RBV PEG + RBV
Discontinuation 35% (n=72) 38% (n=77)
SAE:
IFN + RBV PEG + RBV
SAE 31% (n=64) 31% (n=63)

Improved Outcomes with Increased Ribavirin
Dosing
Peginterferon α-2b vs. Interferon α-2b
n=32 n=32 n=19 n=19n=27 n=27 n=15 n=15
0
10
20
30
40
50
60
70
80
EOT SVR EOT SVR
responserate(%)
PEG (1,5 µg kg qw) INF (3 MIU tiw)
HCV-genotype 1 or 4 HCV-genotype 2 or 3
EOT: p=0.033
SVR: p=0.007
EOT: p=0.914
SVR: p=0.730
Laguno et al. AIDS, 2004.
+ Ribavirin 800 – 1200 mg/d

hypervariable
region
capsid envelope
protein
Protease /
Helicase
RNA-dependent RNA Polymerase
c22
5’
core E1 E2 NS2 NS3
33c
NS4
c-100
NS5a / NS5b
3’
Can Outcomes be Improved with the Addition of
Protease Inhibitors and Other Direct Acting
Antivirals?

Boceprevir andTelaprevir
 Approved and funded
HCV protease inhibitors
for HCV genotype 1
mono-infection based on
substantial improvement
in SVR for treatment
naïve, relapses, partial
responders and null
responders
 Used in combination with
peginterferon alfa-2/
ribavirin
Key Phase III HCV-Mono-
Infection Studies
 Boceprevir
 SPRINT-2: naive GT1
patients
 RESPOND-2: nonresponder
GT1 patients
 Telaprevir
 ADVANCE: naiveGT1
patients
 ILLUMINATE: response-
guided therapy in naive GT1
patients

Boceprevir Plus Peginterferon/Ribavirin for theTreatment of
HCV/HIV Co-Infected Patients
 Two-arm study, double-blinded for BOC, open-label for PEG2b/RBV
 2:1 randomization (experimental: control)
 Boceprevir dose 800 mgTID
 4-week lead-in with PEG2b/RBV for all patients
 PEG-2b 1.5 µg/kg QW; RBV 600-1400 mg/day divided BID
 Control arm patients with HCV-RNA ≥ LLOQ atTW 24 were offered
open-label PEG2b/RBV+BOC via a crossover arm
Weeks 12 24 28 48 72
PEG2b
+RBV
4 wk
Placebo + PEG2b + RBV
44 wk
Boceprevir + PEG2b + RBV
44 wk
Follow-up
SVR-24 wk
Follow-up
SVR-24 wk
PEG2b
+RBV
4 wk
Arm 1
Arm 2
Futility Rules
CROI 2012- Abstract # Q-175

Demographics and Baseline Characteristics
PR
(N=34)
B/PR
(N=64)
Age (years), mean (SD) 45 (9.8) 43 (8.3)
Male, n (%) 22 (65) 46 (72)
Race, n (%)
White
Non-white
28 (82)
6 (18)
52 (81)
12 (19)
Body mass index, mean (SD) 26 (4) 25 (4)
Cirrhosis, n (%) 1 (3) 4 (6)
HCV genotype subtype, n (%)*
1a
1b
22 (65)
10 (29)
42 (66)
15 (23)
HCV RNA level >800,000 IU/mL, n (%) 30 (88) 56 (88)
HIV RNA <50 copies/mL, n (%) 33 (97) 62 (97)
CD4 count (cells/mm3), median (range) 586 (187-1258) 577 (230-1539)
*Subtyping not reported for 9 patients with Genotype 1.

8.8
14.7
23.5
32.4 29.4 26.5
4.7
42.2
59.4
73.4
65.6
60.7
0
20
40
60
80
100
4 8 12 24 EOT SVR12
Treatment Week
PR B/PR
%HCVRNAUndetectable
3/34 3/64 5/34 27/64 8/34 38/64 11/34 47/64
Virologic Response OverTime†
10/34 9/3442/64 37/61
† Three patients undetectable at FW4 have not yet reached FW12 and were not included in SVR12 analysis.

Most Common Adverse Events With a
Difference of ≥10% Between Groups
PR
(N=34)
B/PR
(N=64)
Anemia 26% 41%
Pyrexia 21% 36%
Asthenia 24% 34%
Decreased appetite 18% 34%
Diarrhea 18% 28%
Dysgeusia 15% 28%
Vomiting 15% 28%
Flu-like illness 38% 25%
Neutropenia 6% 19%

Interim Analysis Summary
 HCV-HIV co-infected HCV treatment naïve patients had
high rates of HCV response on BOC
 SVR-12: 61% of patients on B/PR vs. 27% of patients on PR
 Preliminary safety data of B/PR in co-infected patients
showed a profile consistent with that observed in mono-
infected patients

Part A: no ART
Follow-up
PR48
(control)
PR
SVR
Pbo + PR
T/PR TVR + PR Follow-up
SVR
PR
Follow-up
PR48
(control)
PR
SVR
Pbo + PR
T/PR TVR + PR Follow-up
SVR
PR
Part B: ART (EFV/TDF/FTC or ATV/r +TDF + FTC or 3TC)
(EFV)=efavirenz; (TDF)=tenofovir; (FTC)=emtricitabine; (ATV/r)=ritonavir-boosted atazanavir; (3TC)=lamivudine;
(T) TVR=telaprevir 750 mg q8h or 1125 mg q8h (with EFV); Pbo=Placebo; (P) Peg-IFN=pegylated interferon alfa-2a (40 kD) 180 µg/wk; (R)
RBV=ribavirin 800 mg/day or weight-based (1000 mg/day if weight <75 kg, 1200 mg/day for if weight ≥75 kg; France, Germany, n=5 patients)
Roche COBAS® TaqMan® HCV test v2.0, LLOQ of 25 IU/mL, LOD of <10 IU/mL
Telaprevir in Combination with Peginterferon
Alfa-2a/Ribavirin in HCV/HIV Co-infected Patients:
SVR12 Interim Analysis
240 48 72Weeks 12 36 60
SVR12
SVR12
SVR12
SVR12
1:1
2:1
CROI 2012

Patient Demographics and Baseline Characteristics
PartA Part B
NoART EFV/TDF/FTC ATV/r +TDF + FTC or 3TC
T/PR
N=7
PR
N=6
T/PR
N=16
PR
N=8
T/PR
N=15
PR
N=8
Gender, n (%): Male 6 (86) 4 (67) 16 (100) 7 (88) 13 (87) 7 (88)
Caucasian†, n(%)
Black/African American, n(%)
2 (29)
4 (57)
3 (50)
3 (50)
12 (75)
3 (19)
5 (62)
3 (38)
13 (87)
2 (13)
7 (88)
1 (12)
Ethnicity†: Hispanic, n (%) 3 (43) 2 (33) 5 (31) 1 (12) 3 (21) 3 (38)
Age, median years (range) 39 (34-50) 48 (42-65) 48 (31-57) 47 (31-53) 52 (36-59) 39 (26-53)
BMI, median kg/m2 (range) 29 (22-37) 31 (26-37) 24 (21-32) 23 (19-28) 24 (23-33) 25 (22-30)
HCV RNA ≥ 800,000IU/mL**, n (%) 7 (100) 5 (83) 13 (81) 7 (88) 12 (80) 7 (88)
HCV Genotype Subtype*, n (%)
1a
1b
Other
3 (43)
4 (57)
0 (0)
3 (50)
2 (33)
1 (17)
12 (75)
4 (25)
0 (0)
6 (75)
1 (12)
1 (12)
12 (80)
3 (20)
0 (0)
5 (62)
3 (38)
0 (0)
Bridging Fibrosis, n(%)
Cirrhosis, n (%)
1 (14)
0 (0)
0 (0)
0 (0)
2 (12)
2 (12)
1 (12)
0 (0)
0 (0)
0 (0)
1 (12)
0 (0)
HIV RNA median copies/mL (range) 1495
(193-53,450)
267
(25-21,950)
25 (25-25) 25 (25-25) 25 (25-25) 25 (25-25)
CD4+ median cells/mm3 (range) 604
(496-759)
672
(518-1189)
533
(299-984)
514
(323-1034)
514
(254-874)
535
(302-772)
†Race and ethnicity were self-reported *5’NC InnoLipa line probe assay
**Roche COBAS® TaqMan® HCV test v2.0, LLOQ of 25 IU/mL and LLOD of 10-15 IU/mL

PatientswithSVR(%)
No ART EFV/TDF/FTC ATV/r/TDF/FTC Total
n/N = 5/7 11/16 12/15 28/38
T/PR PR
2/6 4/8 4/8 10/22
SVR Rates 12Weeks Post-Treatment
(SVR12*)
71
33
69
50
80
50
74
45
0
10
20
30
40
50
60
70
80
90
100
*Patient was defined as SVR12 if HCV RNA was < LLOQ in the visit window

Events of Special Interest: Overall
Treatment Phase
T/PR
N=38
n (%)
PR
N=22
n/N (%)
Severe rash 0 (0) 0 (0)
Mild and moderate rash 13 (34) 5 (23)
Anemia 7 (18) 4 (18)
Grade 3 hemoglobin
shifts* (7.0-8.9 g/dL)
11 (29) 5 (23)
Use of erythropoietin
stimulating agent
3 (8) 1 (5)
Blood transfusions 4 (11) 1 (5)
•CD4 counts declined in bothT/PR and PR groups; CD4% remained unchanged
*DAIDS HIV-negative scale

Conclusions
 Higher SVR12 rates were observed in chronic genotype 1
HCV/HIV co-infected patients treated with telaprevir
combination treatment
 T/PR 74%
 PR 45%
 In patients treated with telaprevir combination treatment,
overall safety and tolerability profile was comparable to
that previously observed in chronic genotype 1 HCV mono-
infected patients

Interactions Between HCV and HIV PIs
Summary of HealthyVolunteer Studies
-200%
0%
200%
ATVr DRVr FPVr LPVr
Impact on HIV PI Cmin
BOC
-60%
-40%
-20%
0%
ATVr DRVr FPVr LPVr
Impact on HCV AUC
BOC TVR
 Dosing recommendations:
 Boceprevir: coadministration with ritonavir-boosted PIs is not
recommended
 Telaprevir: do not administer with DRVr, FPVr or LPVr;
ongoing evaluation with ATVr
van Heeswijk et al. CROI 2011, #119. Hulskotte et al. CROI 2012, #771LB

Interactions Between HCV DAA & EFV
-20%
0%
20%
AUC Cmin
Impact on EFV PK
BOC TVR 1125 mg q8h TVR 1500 q12h
-60%
-40%
-20%
0%
AUC Cmin
Impact on HCV PK
BOC TVR 750 mg q8h TVR 1125 mg q8h
 Dosing recommendations:
 Boceprevir: co-administration EFV is not recommended
 Telaprevir: use 1125 mgTID with EFV
van Heeswijk et al.CROI 2011, #119. Garg et al. 6th HCV PKWksp 2011, #PK_13.Victrelis Monograph 2011

Statement
 The addition of DAA to IFN-based HCV antiviral therapy
produces a substantial improvement in SVR with minimal
increased sides effects
 Development of other Direct Acting Antivirals holds
promise for additional advances in HIV-HCV co-infection
treatment

Drug Interactions with Directly
Acting Antivirals for HCV
AliceTseng, Pharm.D., FCSHP, AAHIVP
Toronto General Hospital
Faculty of Pharmacy
University ofToronto
Overview and Challenges in
HIV/HCV Co-Infection

Outline
 Understand how the pharmacology of DAAs
contribute to drug interactions
 Highlight important HCV drug interactions
 Outline a strategy for identifying and managing
drug interactions
 Identify pertinent HCV drug interaction resources

Boceprevir andTelaprevir
Pharmacology
Boceprevir Telaprevir
Dosing 800 mg q8h with
food
750 mg q8h with food
(20 g fat)
Substrate CYP3A4, P-gp, AKR CYP3A4, Pgp
Inhibitor 3A4, P-gp 3A4, P-gp, renal
transporters (?)
Inducer No inducing effects in vitro (in vivo?)
potential for interactions with other drugs
• can be clinically significant
• sometimes unpredictable

Interactions Between
HCV & HIV Medications
 Multiple challenges in treating HIV/HCV co-infected
patients
 Additive toxicities:
 anemia: ribavirin, zidovudine, DAAs
 CNS effects: interferon, efavirenz
 Altered concentrations of ARVs and/or DAAs:
  risk of toxicity
  efficacy, potential development of resistance (HIV and/or
HCV)

Telaprevir 750 mg q8h plus Boosted PIs in
HealthyVolunteers
Telaprevir
exposure 
with PI/r
AUC  20-
54%
Cmin  15-
52%
van Heeswijk et al.CROI
2011, #119

Telaprevir 750 mg q8h plus Boosted PIs in
HealthyVolunteers
 Telaprevir
had variable
effect on PIs:
 40-47% 
AUC of
DRVr, FPVr
 n/c with
ATVr, LPVr
 Appropriate
doses not yet
established
van Heeswijk et al.CROI
2011, #119

Two-Way Interaction between
Boceprevir and Boosted PIs
 Interaction studies in healthy volunteers
 Coadministration of boceprevir and ritonavir-boosted
PIs is not recommended
PI Kinetics RTV AUC BOC AUC
Ctrough AUC Cmax
ATVr  49%  35%  25%  34% -
DRVr  59%  44%  36%  27%  32%
LPVr  43%  34%  30%  22%  45%
Hulskotte et al. CROI 2012, #771LB

Interactions Between HCV DAA & NNRTIs
-10 %
-2 9 %
-3 %
9 3 %
-4 0 %
-2 0 %
0 %
2 0 %
4 0 %
6 0 %
8 0 %
10 0 %
Efavirenz Etravirine Rilpivirine
Impact on NNRTI Cmin
Boceprevir
Telaprevir
-44%
-25%
-12%
-25%
-13%
-50%
-40%
-30%
-20%
-10%
0%
Efavirenz Etravirine Rilpivirine
Impact on HCV DAA Cmin
 Dosing recommendations on using HIV non-nucleoside reverse
transcriptase inhibitors (NNRTIs) with HCV directly acting antivirals:
 Efavirenz: avoid with boceprevir, use 1125 mgTID telaprevir
 Etravirine: ? with boceprevir, OK with telaprevir
 Rilpivirine: OK with telaprevir
van Heeswijk et al.CROI 2011, #119. Garg et al. 6th HCV PKWksp 2011, #PK_13.
Victrelis Monograph 2011. Hammond et al. IWCPHT 2012 O-15. Kakuda et al. IWCPHT 2012 O_18

No Clinically Significant Interaction with
Raltegravir and Boceprevir orTelaprevir
Mean Telaprevir PK +/- RAL
Mean Raltegravir PK +/- Telaprevir
de Kanter et al. CROI 2012, #772LB.
van Heeswijk et al. ICAAC 2011, #A1-1738a.
with TVR:
RAL 78% 
Cmin, 26% 
Cmax, 31% 
AUC
Mean Raltegravir PK +/- Boceprevir
 In the presence of
raltegravir, boceprevir
exposures were similar to
historical controls

AntiretroviralTreatment Options in HCV
PIs Avoid with PIr Avoid DRVr, FPVr, LPVr
Possible ATVr???? ATVrOK
Avoid EFV Dose  with EFV
NNRTIs Etravirine (?) Etravirine OK
No data Rilpivirine OK
InSTIs RaltegravirOK
Elvitegravir/cobicistat: no data (???)
Maraviroc No data
potential / MVC; potential benefit on fibrosis?
NRTIs Tenofovir OK
Avoid AZT (anemia)

DAA Interactions with
Other Drug Classes
 Antidepressants
 Methadone
 Benzodiazepines
 Cardiovascular Drugs
 Transplant Drugs

Treatment of Depression in HCV
 Patients with HCV may require antidepressant therapy
 Escitalopram is considered a first-line option
 no interaction with boceprevir
 35%  AUC with telaprevir, may need to titrate dose
 Agents which are partially metabolized via CYP3A4 may
theoretically be  by DAAs
 e.g., desvenlafaxine, venlafaxine, sertraline, mirtazapine,
imiprimine
 combinations not studied, clinical significance unknown
 Low risk of interactions predicted with bupropion, tricyclic
antidepressants, some SSRIs

Methadone Interactions
 Boceprevir interaction:
 R-methadoneAUC 
16%, Cmax  10%; no
withdrawal
 Telaprevir interaction:
 R-methadone Cmin 
31%, Cmax  21%, AUC 
21%, but median unbound
Cmin was unchanged, no
withdrawal Sx
Hulskotte et al. 2012,Van Heeswijk et al. 2011.
 Methadone is metabolized by CYP2B6, CYP2C19 &
CYP3A, 85% protein bound; R-isomer is biologically active
enantiomer

Benzodiazepine Interactions
 Majority are substrates of CYP3A4
 risk for prolonged/excessive sedation
 Oral midazolam & triazolam are contraindicated with
boceprevir and telaprevir
 5 to 9-fold  midazolam AUC with boceprevir or
telaprevir
 IV midazolam: consider  dose, close monitoring for
respiratory depression or prolonged sedation
 Other benzodiazepines:  dose and monitor
 Consider using benzodiazepines that are glucuronidated:
lorazepam, oxazepam, temazepam

Using Statins with Boceprevir or
Telaprevir
Lovastatin,
Simvastatin
CONTRAINDICATED
Atorvastatin May need to  atorvastatin
dose; do not exceed >20 mg/d
CONTRAINDICATED
Pravastatin Start with recommended dose
and monitor for toxicity.
Possible  in statin; use
with caution.
Rosuvastatin,
Fluvastatin
Possible  in statin; use with caution.
Victrelis & Incivek Product Monographs, 2011; FDA HIV/AIDS Update, 2012.
 Use lowest statin dose and titrate slowly to response

Effect of Steady-StateTelaprevir on the
Pharmacokinetics of Amlodipine 5 mg
Calcium channel
blockers (CCBs)
Amlodipine, diltiazem, fel
odipine, nifedipine, nicard
apine, verapamil are
CYP3A4 substrates
Concentrations may be 
by boceprevir or telaprevir
Use with caution, clinical
monitoring
Consider dose reduction
Lee et al. AntimicrobAgents Chemother 2011.
 amlodipineAUC  179%
 monitor for dose-related toxicity

Interactions between DAAs and
Transplant Drugs
 Cyclosporine & tacrolimus are CYP3A4 substrates; significant
 concentrations with DAAs:
 cyclosporine: AUC  2.7-fold with boceprevir,  4.64-fold with
telaprevir
 tacrolimus: AUC  17.1-fold with boceprevir,  70.3-fold with
telaprevir
  CsA andTAC dosing with telaprevir coadministration:
 CsA:  from 200 mg to 25 mg daily (n=7)
 TAC:  to 50% dose given weekly (n=7)
Hulskotte et al. HEP DART 2011, poster 123. Garg et al. Hepatology, 2011. Mantry et al. HEP DART 2011, #90.
Kwo et al. EASL 2012, #202.

Drugs Contraindicated with Boceprevir and
Telaprevir (1)
1-adrenoreceptor
antagonist
alfuzosin hypotension, cardiac
arrhythmia
antiarrhythmics Quinidine,
propafenone,
amiodarone.
Flecainide (TVR)
serious/life-threatening
cardiac arrhythmia
antimycobacterials Rifampin Loss of virologic response
Ergot derivatives Acute ergot toxicity
Herbal product St. John’s wort Loss of virologic response
Statins Lovastatin,
simvastatin.
Atorvastatin (TVR)
Myopathy including
rhabdomyolysis
neuroleptic Pimozide serious/life-threatening
cardiac arrhythmia
Victrelis & Incivek Product Monographs, 2011

Drugs Contraindicated with Boceprevir and
Telaprevir (2)
PDE-5 inhibitor sildenafil.
tadalafil (BOC);
vardenafil (TVR)
Visual abnormalities, hypotension,
prolonged erection, syncope
Sedatives/
hypnotics
oral midazolam,
triazolam
Increased sedation or respiratory
depression
Other cisapride, astemizole,
terfenadine
serious/life-threatening cardiac
arrhythmia
Anticonvulsants
(BOC)
carbamazepine,
phenytoin,
phenobarbital
Loss of virologic response
OC (BOC) drospirenone hyperkalemia
Aldosterone
antagonist (TVR)
eplerenone hyperkalemia
Triptans (TVR) eletriptan Coronary artery vasospasm, MI,
vent. tachycardia, VF
Victrelis & Incivek Product Monographs, 2011.

Summary
 Potential for numerous interactions between DAAs and
ARVs, as well as agents prescribed by other providers
 challenge in treating HIV/HCV coinfected patients, particularly
in context of earlier cART initiation, aging population and
management of comorbidities
 Steps to minimizing/managing interactions:
 ensure medication records are up to date at each visit
 utilize pertinent drug interaction resources to identify combinations
of potential concern
 consult with physicians & pharmacists with expertise in HIV and HCV
 institute therapeutic plan with close monitoring

HIV & HCV
Drug Interaction Resources
 Interactions in HCV and HIV:
 Kiser J et al. Hepatology 2012;55:1620-8.
 Tseng & Foisy. Curr Infect Dis Rep 2012;14:67-82.
 Internet
 Toronto General Hospital Immunodeficiency Clinic;
www.hivclinic.ca, www.hcvdruginfo.ca
 Liverpool Pharmacology Group; www.hep-
druginteractions.org

David Fletcher, MD
Department of Medicine
University ofToronto
Complicated cases

CASE 1
 54 yr/o man
 HIV positive 8 yrs ago
 Tenofovir/FTC/RTV/Atazanavir x 4 yrs
 Previously documented NNRTI resistance with
Y181C, G190A,and mixed m184v/wt
 CD4 320 HIVViral Load<40

CASE 1
 Genotype 1a Hepatitis C biopsy proven cirrhosis
 Compensated and clinically stable
 Previous therapy in 2009 with Peg INF/1200mg RBV daily
resulted in a null response by history from the patient

CASE 1
Patient is interested in a retrial of therapy for
Hepatitis C with the new direct acting antiviral agents
 Would you offer treatment?
 Chance of cure?
 Which 3rd agent would you choose and why?
 Does patient’s antiretroviral history play a role in 3rd agent
choice?
 Is there a role for a 4 week lead in here regardless of agent
chosen and if so…why?

CASE 1
It was decided to move forwards with Peg INF/
1200mg RBV/Telaprevir
 Is it necessary to change current ARVs?
 Would it be necessary to change ARVs if Boceprevir was
chosen?...to what?

CASE 1
Peg INF/1200mg RBV/Telaprevir…no lead in
performed
 Week 0 HCVRNA 3.7 x 10e7
 Week 4 HCVRNA detectable but<12
 Would you continue?
 Are you concerned about the result?
 When would you do the next HCVRNA?

CASE 1
It was decided to continue with Peg INF/1200mg
RBV/Telaprevir and HCVRNA rechecked
 Week 6 HCVRNA <12
 Would you continue?

CASE 1
Peg INF/1200mg RBV/Telaprevir
 Week 0 HB 140
 Week 2 HB 125
 Week 4 HB 109
 Week 6 HB 99…symptomatic
 How would you manage anemia?

CASE 1
 Week 6 HCVRNA <12 HB 99 (symptoms)
 Week 8 HCVRNA <12 HB 98 (less symptomatic)
 What would you do?
 How would you further manage anemia

CASE 1
 Week 12 HCVRNA detectable but <12 HB 103
 When would you do your next HCVRNA?

CASE 1
Peg INF/RBV re-increased to 1200mg
 Week 4 HCVRNA detectable but <12
 Week 14 HCVRNA <12 HB 101

CASE 1
Peg INF/1200mg RBV
 How much longer would you treat?
 When would you do your next HCVRNA?

CASE 1
Peg INF/1200mg RBV
 Are we finished therapy?

CASE 1
An additional 24 weeks of PEG INF/RBV (for a total of
72 weeks of therapy) was offered to the patient given
the existence of cirrhosis and ?slow HCVRNA clearance
as evidenced by a detectable HCVRNA at week 4 and
12
Week 12 and 24 HCVRNA post 72 weeks of therapy
were undetectable!

CASE 2
 52 yo man
 HIV positive 5 yrs ago
 CAD with previous MI 3 yrs ago/Hypertensive/Hypothyroidism
 Tenofovir/FTC/Raltegravir x 4 yrs
 CD4 700 HIVViral Load<40

CASE 2
 Hypercholesterolemia and Hypertriglyceridemia on
combination therapy with Atorvastatin 80mg/day and
Fenofibrate 145mg/day
 Hypertension controlled on Amlodipine 10mg/day
 Hypothyroidism controlled on 0.125 mg L-Thyroxine

CASE 2
 Genotype 1a chronic hepatitis C
 Naïve to therapy
 F2-3/4 scarring
 Ready to start triple therapy with PEG
INF/RBV/Boceprevir
 Atorvastatin decreased to 40mg/day
 Baseline HCVRNA 1.66X10E6

CASE 2
 Week 0 HCVRNA 1.66x10E6
 Week 4 HCVRNA (lead in) 2.37x 10E2
 At week 10 begins to feel tired/weak/constipated/muscle
cramping
 TSH noted to be 18.91…L-T4 increased to 0.15mg/d in
response

CASE 2
 At week 11 notes increasingly prominent myalgias, more
predominant post interferon injection but lasting all
week long as opposed to a few hrs post injection, along
with increasing weakness
 Hb stable at 105g/l over last few weeks with RBV dose
reduction to 600mg/d
 AST noted to be increasing while ALT has been
normalizing over the last few weeks…also increasing
swelling of ankles
 ?Cause…Hepatic Decompensation?

CASE 2
 CK measured at 83,700
 BP noted to be low at 90/55 and swelling of ankles worsened
now to mid calf…no ascites noted clinically
 Cause?

CASE 2
 Atorvastatin and Fenofibrate discontinued!!!
 CK fell over the next few weeks as did AST
 The symptomatic myalgias and weakness improved over the
subsequent month
 Amlodipine discontinued…BP normalized to 130/80 and
ankle swelling disappeared over the next month

FutureTrials of Hepatitis C
Therapy in the HIV Co-infected
Stephen D. Shafran, MD, FRCPC, FACP
Department of Medicine, Division of Infectious Diseases
University of Alberta

Ongoing ClinicalTrials of HCVTherapy
in the HIV Co-infected
 As of November 2012, the following regimens are under
ongoing study:
 IFN-containing (only for HCV genotype 1)
 PegIFN-2a + RBV* + NS3 Protease Inhibitors
 PegIFN-2a + RBV + telaprevir
 PegIFN-2a + RBV + simeprevir
 PegIFN-2a + RBV + faldaprevir
 PegIFN-2a + RBV + NS5A Inhibitor
 PegIFN-2a + RBV + daclatasvir
 IFN-sparing (only for HCV genotypes 2 & 3)
 Sofosbuvir (nucleotide polymerase inhibitor) + RBV
www.clinicaltrials.gov* RBV = ribavirin

Two Ongoing Studies of PegIFN-2a + RBV +
Telaprevir in the HIV Co-Infected
Trial name Vertex 115 INSIGHT
Trial identifier NCT01467479 NCT01513941
Study design Open-label Open-label
No of subjects 160 150
HCV patient types GT1 Naïve, relapsers, partial responders, null responders
Telaprevir dosing* 1125 mg BID x 12 wk 750 mgTID x 12 wk
Study locations USA,Canada, Spain, Germany Europe,Australia, Brazil
Duration of PR RGT (24 or 48 wk) in naives and relapsers;
48 wk in partials and nulls
RBV dose 800 mg/d
ART Must be on suppressive ART
Baseline CD4 > 300 cells/mm3
Study status Fully enrolled Enrolling
SVR12 expected Q3 2014 Q3 2014
*Telaprevir dosed 1125 mgTID in patients receiving efavirenz www.clinicaltrials.gov

Ongoing Study of PegIFN-2a + RBV +
Simeprevir in the HIV Co-Infected
Trial name C212
Trial identifier NCT01479868
Study design Open-label
No of subjects 107
HCV patient types GT1 Naïve, relapsers, partial responders, null
responders
Simeprevir dosing 150 mg QD x 12 wk
Study locations USA, Europe, Canada
Duration of PR RGT (24 or 48 wk) in naives and relapsers; 48 wk in
partials/nulls/cirrhotics
RBV dose 800 mg/d
ART and CD4 CD4 > 300 on suppressive ART; or not on ART with
CD4 > 500 and HIV RNA <100,000
Study status Fully enrolled
SVR12 expected Q4 2014
www.clinicaltrials.gov

Faldaprevir in the HIV Co-Infected
Trial name STARTverso4
Study design open-label with multiple randomizations
No of subjects 306
HCV patient types GT1 Naïve, relapsers
Faldaprevir dosing 120 mg or 240 mg QD
Study locations USA, Europe, Brazil
Duration of PR RGT in naives and relapsers; 48 wk in
partials/nulls/cirrhotics
RBV dose 1000/1200 mg/d
ART and CD4 CD4 > 300 on suppressive ART, OR not on ART with
CD4 > 500 and pVL <100,000
Study status Fully enrolled

PegIFN-2a + RBV + Faldaprevir for HCV GT1 in HCV
Treatment-Naïve and Relapser Patients with HIV Co-infection
Week 24 Week 48Week 12
Faldaprevir
240 mg QD +
PegIFN/RBV
PegIFN/RBV
Faldaprevir
240 mg QD +
PegIFN/RBV
Randomization
(1:1)
ETS patients are re-randomized (1:1)
No ETS = 48 weeks PegIFN/RBV
Week 120
Faldaprevir
120 mg QD + PegIFN/RBV
PegIFN/RBV
PegIFN/RBV
PegIFN/RBV
Day 1
Randomization
(1:1)
Follow-up:
up toWeek 120
ETS (early treatment response):
HCV RNA <25 IU/mL, detectable
or not atWeek 4 and <25 IU/mL,
undetectable atWeek 8
* Patients directly assigned to the 240 mg dose group if receiving efavirenz and
to the 120 mg dose group if receiving darunavir/ritonavir or atazanavir/ritonavir
*

Daclatasvir in the HIV Co-Infected
Trial name COMMAND-HIV
Study design open-label
No of subjects 300
HCV patient types GT1 Naïve
Daclatasvir dosing 30 mg QD (ATZ/r, LPV/r or DRV/r), 60 mg QD (RAL, RIL
or no ART) or 90 mg QD (EFV or NVP), all for 24
weeks
Study locations USA, Europe, Brazil
Duration of PR RGT (24 or 48 wks)
RBV dose 1000/1200 mg/d
ART and CD4 CD4 > 100 on suppressive ART,
or not onART with CD4 > 350
Study status GT 1a capped. Still enrollingGT1b.

Ongoing Study of Sofosbuvir + RBV
in the HIV Co-Infected
Trial name
Study design open-label
No of subjects 115
HCV patient types GT 2 and 3 Naïve and PR failures
Sofosbuvir dosing 400 mg QD x 12 wk (naïve) or 24 wk (TF)
RBV dosing 1000/1200 mg/d x 12 wk (naïve) or 24 wks (TF)
Study locations USA
ART and CD4 CD4 > 200 on suppressive ART,
or not on ART with CD4 > 500
Study status Enrolling

FutureTrials of Anti-HCVTherapy Anticipated
in the HIV Co-infected
 Following completion of DDI studies identifying compatible
ARVs, the following promising IFN-free anti-HCV regimens in
the HCV-mono-infected may be tested in the HIV+
population:
 Sofosbuvir + RBV (likely GT 2 and 3 only)
 Sofosbuvir + NS5A inhibitor (likely pangenotypic)
 SOF + GS-5885 fixed-dose combination (FDC)
 SOF + Daclatasvir
 NS3 + NNI + RBV (GT1 only)
 Faldaprevr + BI-207127 + RBV in GT1b or GT1a/IL-28BCC
 Telaprevir +VX-222 + RBV
 NS3 + NNI + NS5A ± RBV
 ABT-450/ABT-267/RTV (FDC) + ABT-333 ± RBV

HCV Infection in Marginalized
Populations
Brian Conway, MD, FRCPC
Vancouver Infectious Diseases Centre
(VIDC)

IDUs will drive the future HCV epidemic in
Canada
 300,000 HCV-infected
Canadians, including over 180,000 IDUs
(60% of prevalent cases)
 14,000 new cases are diagnosed each
year, including over 11,000 in IDUs
(78% of incident cases)
 Traditional medical models (diagnosis-
treatment-prognosis) will NOT apply to
their engagement in care and successful
implementation of successful antiviral
therapy
Remis, Health Canada, 2004. Fischer et al. Can J Pub Health, 2006. Zou.Can J Pub Health, 2003.

HCVTreatment Uptake Overall
S. Mehta, with permission
Overall treatment uptake is low in most places…..

Treatment Uptake in HIV-HCV Co-infection
N Cohort HCV
Treatment
Uptake
Canada (Vancouver)
(Grebely et al. JViral Hep 2008)
1,361 Urban clinic of HCV &
HIV/HCV co-infected
patients
1.1%
United States (Baltimore)
(Mehta et al. AIDS 2006)
845 Urban clinic of HIV/HCV
co-infected patients
3.4%
Australia
(NCHECR 2005)
2,500 Needle exchange 4.0%
NCHECR, 2003. Australia.
Grebely et al. J Hepatology, 2006.

Barriers to HCVTreatment
Patient Barriers
• Poor awareness/ education
• Lack of symptoms
• Competing health priorities (HIV, psychiatric)
• Competing social priorities (housing, substance use,
financial)
• Fear of side effects
Provider Barriers
• Poor awareness/education
• Reticence to treat IDUs
• Lack of providers, especially in remote
communities
• Focus on HIV
Structural Barriers
• Lack of infrastructure/multidisciplinary support
• Segregated services
• Provincial regulations
• Cost

Example: Overcoming structural barriers:
Integrated care / co-location of HCV & Substance abuse treatment
Co-location of HCV care with
methadone maintenance has been
associated with favorable outcomes
(One-stop shopping)
Integrated services for
HCV, addiction, mental health and
psychosocial problems
Some programs Incorporate peer
educators
• Peer educators are patients who have
successfully completed HCV treatment
• Peers lead support groups with medical
providers
• Provide support through all stages
from HCV screening to treatment
Sylvestre 2007; Harris 2010; Litwin 2007; Edllin 2006; Grebely 2010. S. Mehta, with permission

Canadian situation
 2007 Canadian consensus guideline reads: An
appropriately funded multidisciplinary effort is required to
improve care strategies for HCV infected IDU. Antiviral
therapy should be considered in selected patients in whom
HCV related morbidity & mortality will become relevant.
 BUT 80% of Canadian physicians specialized in treating
viral hepatitis would not treat active drug users
Myles et al.Can J Gastroenterology, 2011

Academic & Community Partnership Care
Model
 In the community
 Community & Academic Partnership
 ONE STOP SHOP
 Multidisciplinary
 Physicians (addiction & hepatology)
 Nurses
 Outreach workers
 Research assistants
 Culture of research & excellence

Patient Characteristics and Response Rates
 Mean age 43, 83% male, 55% genotype 2/3
 Early discontinuation - 11 patients (28%)
 Treatment-limiting adverse events – 5 patients (13%)
 nausea/vomiting, tinnitus, neutropenia, depression, anemia
 Illicit drug use – 6 patients (15%)
ETR SVR
0
20
40
60
80
100
n=40 n=40
70%
55%
%Response
Grebely et al. J Gastroenterology and Hepatology, 2007.

Impact of Illicit Drug Use on Response
 35% used illicit drugs in the last 6 months
 48% used illicit drugs during treatment
 10 (25%) used occasionally (monthly or once/twice)
 9 (23%) used frequently (every day/every other day)
>6 mos 6 mos None Any Occ Freq
0
20
40
60
80
100
n=26 n=21n=14
50% 53%
80%
64%
n=19
Drug Abstinence Illicit Drug Use
During Treatment
57%
n=10 n=9
22%
%SVR
Grebely et al. J Gastroenterology and Hepatology, 2007.

Occurrence ofViremia in IDUs
 After adjusting for potential confounders:
 Individuals with viral clearance were 4 times less likely to develop infection
than those infected for the first time
 THESE DATA MAY NOT (OR MAY) APPLYTOTREATMENT-INDUCED
VIROLOGICCLEARANCE
Grebely et al. Hepatology, 2006.

VIDC Baseline Characteristics
Characteristic n (%)
Total treatment cases, (n) 302
Median Age in yrs (Range) 53 (34-70)
Female, n (%) 44 (15)
HIV co-infection, n (%) 43 (14)
HCV genotype, n (%)
Genotype 1
Genotype 2/3
189 (63)
113 (37)
Treatment experience, n (%)
Naïve
Experienced
252 (83)
50 (17)
Liver Cirrhosis, n (%)
History of recent IDU, n (%)
On methadone maintenance therapy, n (%)
33 (11)
302 (100)
211 (70)

Number of patients initiating treatment
N=302
14 14
10 12
39
26
44
61
55
27
0
10
20
30
40
50
60
70
2003 2004 2005 2006 2007 2008 2009 2010 2011 2012
Year of Initiation

SVR rates in all treated and evaluable
patients N=251
45
65
53
42
60
47
0
10
20
30
40
50
60
70
Genotype 1 Genotype 2/3 Overall
All HIV Co-infected

Treatment Discontinuation in all treated and
evaluable patients; n=251
Genotype 1
N=155
Genotype 2/3
N=96
Overall
N=251
CompletedTherapy 95 (61%) 72 (75%) 167 (67%)
Discontinued due to:
• Lack of Response
• DrugToxicity
• Non-adherence / drug
relapse
60 (39%)
37 (24%)
13 (8%)
10 (7%)
24 (25%)
7 (7%)
14 (15%)
3 (3%)
84 (33%)
44 (17%)
27 (11%)
13 (5%)

HCVTreatment Discontinuation Rates in
IDUs vs. non-IDUs
 Lee et al. (Liver Int. 1270-77, 2012)
 8853 courses of Peg-IFN-2a in non-IDUs
 68.3% completion rate
 10.3% discontinuation for toxicity

Conclusions
 HCV infection can be treated successfully in IDUs with
response rates and patterns of treatment discontinuation
similar to those seen in other populations, independent of
HIV co-infection status.
 As reflected in the 2012 Canadian guidelines for the
treatment of HCV infection, IDUs should be considered for
HCV therapy when this is medically indicated,
preferentially within the context of multidisciplinary
community-based models for the delivery of health care
where state-of-the-art expertise for the management of
HCV infection is available.

EnTEnTE
 Engage:Take people who are not involved in their own
health care and get them involved
 Test: Offer HCV testing in a setting favouring patient
engagement
 Engage: Once a test result is available, use it to establish a
long-term clinical relationship
 Treat: Optimize conditions to achieve SVR
 Engage: Towards a long-term solution to social inequality

THE (NEAR) FUTURE
 Test all marginalized populations for the presence of HCV
infection
 Select “optimal” patients for HCV treatment NOW
 Continue to engage non-treated patients in ongoing
models of care
 Seek &Treat models MUST be developed for HCV, with a
realistic expectation of disease eradication in selected
communities, given the increasing efficacy of available
treatment modalities

HIV / HCV co-infection
Through the eyes of a co-infected
hemophiliac
I.D.

History-The HCV Diagnosis
 More bad news delivered on the heels of an HIV diagnosis.
 I attend funerals for others I knew through the hemophilia
clinic, lost to HIV.
 My physician is relieved that I take the news so well. It’s
the early 90’s & my HIV is raging, CD4 falling, & no
treatment is offered. In this context I consider if an HCV
infection will even matter? Surely HIV will take me before
HCV gets a chance.
 I view treatment as pointless.

The Genetic Lottery
 My physician tells me little is known about predicting
progression.
 I am told that approximately 20% clear the virus
spontaneously & many live a full life unaware they carry
the virus. Did I win the genetic lottery?
 Later I receive PCR and genotype information,….
Sorry,Type 1a & PCR pos, not a winner this time.

OPTIONS
 Do I stick my head in the sand and hope to be a slow or
non-progressor?......I remember my previous genetic
lottery result.
 Ifn + Rib as a combination arrives - I watch friends suffer
and hear stories of very limited success. My HIV is not yet
under control, & decide HCV treatment is not for me – at
least not yet.
 I continue to wonder if my HCV diagnosis will really matter
in the context of my HIV infection. I am told I could wait &
choose to do so, but for how long?

Evolution
 HAART arrives & HIV treatment improves. My general health
improves. My HIV is finally under control.
 My outlook on life changes from planning no more than 2 years
ahead to looking 5years ahead but I’m afraid of another set back.
 I hear talk in the hemophilia community that friends are not dying
from HIV anymore, HCV is now taking them.
 Another evolution in HCV treatment arrives - Peg Ifn + Rib.The viral
clearance numbers are better.Treatment now looks possible
although the side effects seem daunting.
 I am told age is a determinant of success & I am approaching 40. My
liver enzymes >3xULN, I take the chance.

EarlyTreatment - Peg Ifn Rib
 Treatment is required for a full year due to geno-type, it’s
now 2002 - I feel I can do this!
 I am unable to access a hepatologist but treatment is
offered through my HIV doctor.
 Treatment costs are high but I still have private drug
coverage – I feel lucky, but what about the others?
 I discuss side effects with my physician and he puts me at
ease, assures me that not everyone experiences harsh
effects to treatment – I am now ready!

EarlyTreatment – Initial Side Effects
 I take the first dose at the HIV clinic and become ill on the
drive home. I crawl into bed. Sweats, chills, high fever,
nausea, pounding head, lower back pain, they said flu like,
but this is much more.What exactly did I sign on to?
 I panic, was I having an unexpected reaction? I want to call
someone to ask if this is going to get worse but it’s now
after 5pm and no one is available to answer.

EarlyTreatment continues
 Difficult to eat & unable to enjoy the sun & heat during the
summer.Thirsty, always thirsty – a small price to pay.
 Side effects remain strong for the first 6mos then
gradually reduce.Weight loss, mood changes & depression
seem the worst.
 Interim results are in & it looks like I will clear the virus –
hooray!
 Many mornings my wife leaves for work while I remain on
the bathroom floor – still thinking it will all be worth it.

What could have improved the
treatment experience?
* Support *
Having someone available by phone in the off hours if I had
questions or needed help dealing with a side effect.
Being connected to someone else that was previously
successful for peer support.

After treatment – Peg ifn + Rib
 Treatment ends & my body weight comes back, with a vengeance, I will
have to be careful now. It’s a problem I actually welcome after experiencing
HIV wasting.
 I still have trouble tolerating heat and sun – but it seems a small price to pay.
 My liver enzymes have fallen to almost normal levels, I feel good about the
sacrifice.
 6 mos out I am retested for HCV and find that the virus has returned. I no
longer feel lucky.
 Other than longer terms of Peg-ifn treatment no other options are available.
I am told I can afford to wait for newer treatments but there are none on the
horizon.
 I continue attend the funerals for others I knew through the hemophilia
clinic, now lost to HCV instead of HIV.

The Hepatologist
 A few years after treatment failure I am assigned a hepatologist.
 There are still no treatment options to offer other than more peg-ifn +
Rib. He speaks of new treatment concepts using protease inhibitors
that are far off but coming.
 Closer monitoring with Fibroscan and ultrasound begin.
 I am still sick, but now well documented.
 Results indicate I am one of the lucky ones that can wait for newer
treatments to arrive.
 No clear strategy is offered for taking care of my liver in the interim
other than advice to increase my coffee intake, avoid alcohol, be
careful with my diet and try to exercise.
 I sympathize with my hepatologist for having so few tools to fight
HCV and I am reminded again of the early days of HIV infection.

Where do affected persons go for
information and support
 Our HIV Physicians & Hepatologists
 AIDS Service Organizations (CATIE is probably the best source)
 Canadian Hemophilia Society
 Provincial/Regional HepC organizations where available (i.e.
HepCBC)
 The Internet
 The Canadian Liver foundation
 Other affected persons

The landscape today
Effective treatment may finally be just over the horizon – but
for who?
 Fast Forward 10 years from my attempt at treatment with peg-
ifn + Rib and HCV treatment is rapidly evolving, similar in many
ways to the early days of HIV.
 From the patients perspective an alphabet soup of new
medications are now making their way through the pipeline.
The results look promising.
 We just need to hold on long enough.

Access to the latest available treatment
Telaprevir & Boceprevir
 Approved by Health Canada
 Doctors & most patients are aware of the improvement in viral
clearance rates and there is good reason to be excited about this
data.
 These new combinations provide increased rates of viral clearance
but are still linked to a high degree of treatment side effects.
 Although the latest data is promising there remains a lack of trials
in co-infected persons, and because of this treatments are not yet
indicated for this group.

Are the people most in need getting
access to the latest treatments?
 Access toTelaprevir & Boceprevir differs by Province,
formularies are not uniform – What happened to Universal
Health Care?
 For example Ontario provides access to Boceprevir only through
the Exceptional Access Program but attaches a list of conditions
to restrict use.The reality is that although the drug is available
access is being rationed, especially for those most in need.
 Provincial governments should not get a free ride on heels of
positive data for new treatment combinations by on one hand
making them available through EAP & on the other rationing
access through the use of limitations like “co-infected patients
are not eligible”.

Transplantation
 Livers are in short supply
 To a hemophiliac in need of a liver this is the holy grail. A
successful liver transplant represents a win for all sides as it
cures hemophilia and potentially reduces a significant cost
burden to the system for factor replacement therapy going
forward. Unfortunately this option remains only a mirage for
not just HCV+ hemophiliacs but all co-infected patients.
 There remains a reluctance within transplant centres here in
Canada to offer organs to people co-infected – social stigma?
 Co-infected persons have been known to die, unable to just
get on the transplant list let alone receive a transplant – is
this just?

What’s different
 When compared to early advances in HIV treatment what appears
different is an absence of strong patient and researcher based
advocacy dedicated to HCV patients.
 While some exist, community based organizations dedicated to
HCV are few and underfunded compared to HIV resulting in a void in
care and support
 HIV ASO’s provide information & have included some advocacy
efforts due to the overlap of co-infected patients but is it enough?
 Only a small number of liver specialists exist in Canada, can patients
get access to specialized care?
 No organization appears dedicated to pursuing HCV clinical
research questions in Canada in the same way we handle HIV.

What’s needed
 Improved access to the latest treatments, across all
Provinces. Stop excluding those most in need.
 Research into developing treatment strategies to preserve
the liver for patients currently in a holding pattern that need
or want to wait for future treatments.
 Provide stable funding both Federally and Provincially for
organizations supporting HCV infected persons. Delays in
renewing funding agreements has put at risk the very
existence of many organizations. PHAC has not lived up to
the ongoing funding promise made by the Minister of Health
in 2008.

What’s needed (continued)
 Begin to provide access to transplants for co-infected patients here
in Canada.
 Begin to explore the option of using livers from HIV infected
donors in infected persons as a life saving measure here in Canada.
 Increase research focusing on the latest HCV treatments in co-
infected populations as well as those previously experiencing
treatment failure.
 Wider circulation of information and how to access clinical trials
combined with encouragement and support for University and
Industry research from government. Clinical trials in rural centres
are needed.

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